Limitations of the Wittig-Horner-type annulation of fluorobutenolide moiety to 3-hydroxyquinoline-2,4(2H,3H)-diones. Novel modifications of the Perkow reaction including fluorinated acyloxy leaving groups

Tetrahedron

Volumn 63, Issue 42, 2007, Pages 10549-10561

  Pomeisl, Karel ^a   Kvíčala, Jaroslav ^b   Paleta, Oldřich ^b   Klásek, Antonín ^c   Kafka, Stanislav ^c   Kubelka, Vladislav ^d   Havlíček, Jaroslav ^d   Čejka, Jan ^b  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

^b INSTITUTE OF CHEMICAL TECHNOLOGY   (Czech Republic)

^c TOMAS BATA UNIVERSITY IN ZLIN   (Czech Republic)

^d Zentiva Prague   (Czech Republic)

Author keywords

3 Halogenoacyloxyquinoline 2,4(1H,3H) diones; 19F NMR reaction profile; Breast carcinoma; But 2 enolide, Perkow reaction; Chronic myeloid leukemia; Cytostatic activity; Fluorofuranone; Lithium 2 (diethoxyphosphoryl) 2 fluoroacetate; Wittig Horner synthesis

Indexed keywords

3 (FLUOROACYLOXY)QUINOLINE 2,4(1H,3H) DIONE DERIVATIVE; 3 HYDROXYQUINOLINE 2,4(2H,3H) DIONE DERIVATIVE; 4 ETHOXYQUINOLIN 2(1H) ONE; BUTENOLIDE; CARBOXYLIC ACID; FLUORINE DERIVATIVE; FLUOROBUTENOLIDE; FLUOROCARBOXYLATE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANNULATION REACTION; ARTICLE; HORNER REACTION; PRIORITY JOURNAL;

EID: 34548297977     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.07.058     Document Type: Article

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